Effect of nitazoxanide on albendazole pharmacokinetics in cerebrospinal fluid and plasma in rats

Bibliographic Details
Title: Effect of nitazoxanide on albendazole pharmacokinetics in cerebrospinal fluid and plasma in rats
Authors: María Isabel Ruiz-Olmedo, Iliana González-Hernández, Francisca Palomares-Alonso, Javier Franco-Pérez, María de Lourdes González F., Helgi Jung-Cook
Source: Saudi Pharmaceutical Journal, Vol 25, Iss 3, Pp 413-418 (2017)
Publisher Information: Elsevier, 2017.
Publication Year: 2017
Collection: LCC:Therapeutics. Pharmacology
Subject Terms: Albendazole, Albendazole sulfoxide, Nitazoxanide, Tizoxanide, Cerebrospinal fluid, Pharmacokinetics, Therapeutics. Pharmacology, RM1-950
More Details: Background: Although albendazole is the drug-of-choice for the treatment of neurocysticercosis, its efficacy is limited due to its low bioavailability. An alternative for optimizing pharmacological treatment is through drug combinations. In vitro studies have shown that nitazoxanide and tizoxanide (the active metabolite of nitazoxanide) exhibit cysticidal activity and that the combination of tizoxanide with albendazole sulfoxide (the active metabolite of albendazole) produced an additive effect. Objectives: (1) To assess the concentration profile of tizoxanide in plasma and in cerebrospinal fluid; and (2) to evaluate the influence of nitazoxanide on the pharmacokinetics of albendazole in plasma and in cerebrospinal fluid. Methods: Two different studies were conducted. In study 1, 10 male Sprague-Dawley rats received a single oral dose of 7.5 mg/kg of nitazoxanide and serial blood and cerebrospinal fluid samples were collected over a period of 4 h. In study 2, 38 healthy male Sprague-Dawley rats were randomly divided into two groups: one of these received a single dose of albendazole (15 mg/kg) and, in the other group, albendazole (15 mg/kg) was co-administered with nitazoxanide (7.5 mg/kg). Plasma and cerebrospinal fluid samples were collected from 0 to 16 h after administration. Albendazole sulfoxide and tizoxanide levels were assayed by using HPLC or LC/MS techniques. Results: In study 1, tizoxanide reached a maximum plasma concentration of 244.42 ± 31.98 ng/mL at 0.25 h; however, in cerebrospinal fluid, this could be detected only at 0.5 h, and levels were below the quantification limit (10 ng/mL). These data indicate low permeation of tizoxanide into the blood brain barrier. In study 2, Cmax, the area under the curve, and the mean residence time of albendazole sulfoxide in plasma and cerebrospinal fluid were not affected by co-administration with nitazoxanide. Conclusion: The results of the present study indicate that in rats at the applied doses, tizoxanide does not permeate into the cerebrospinal fluid. Furthermore, nitazoxanide does not appear to alter significantly the pharmacokinetics of albendazole in plasma or in cerebrospinal fluid.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1319-0164
Relation: http://www.sciencedirect.com/science/article/pii/S1319016416300974; https://doaj.org/toc/1319-0164
DOI: 10.1016/j.jsps.2016.09.005
Access URL: https://doaj.org/article/a8d98bd1f67f4c8d863ea4a236f74d1b
Accession Number: edsdoj.8d98bd1f67f4c8d863ea4a236f74d1b
Database: Directory of Open Access Journals
More Details
ISSN:13190164
DOI:10.1016/j.jsps.2016.09.005
Published in:Saudi Pharmaceutical Journal
Language:English